- Are you an experienced Quality & Continuous Improvement Coordinator who is flexible, detail-oriented, and thrives on solving tough problems? We are looking for an individual to champion the quality of our client's products using both automated and manual tests, reporting and verifying defects. If you are looking to stand out in your field this may be the opportunity for you.salary: $55,000 - $65,000 per yearshift: Firstwork hours: 8 AM - 5 PMeducAre you an experienced Quality & Continuous Improvement Coordinator who is flexible, detail-oriented, and thrives on solving tough problems? We are looking for an individual to champion the quality of our client's products using both automated and manual tests, reporting and verifying defects. If you are looking to stand out in your field this may be the opportunity for you.salary: $55,000 - $65,000 per yearshift: Firstwork hours: 8 AM - 5 PMeduc
- About Us: Join our team in the medical device/pharmaceutical industry, where we prioritize product quality and regulatory compliance. We are seeking a dedicated QA Specialist to support our Quality Management System (QMS) and ensure the highest standards of quality. Key Responsibilities: Ensure compliance with company policies and procedures. Support production with process validation and equipment qualifications. Assist with complaint investigations, roAbout Us: Join our team in the medical device/pharmaceutical industry, where we prioritize product quality and regulatory compliance. We are seeking a dedicated QA Specialist to support our Quality Management System (QMS) and ensure the highest standards of quality. Key Responsibilities: Ensure compliance with company policies and procedures. Support production with process validation and equipment qualifications. Assist with complaint investigations, ro
- We are seeking a Quality Validation Manager to join our team, responsible for ensuring the compliance of manufacturing equipment, processes, and sterilization protocols with industry regulations. This role involves developing, executing, and maintaining IQ/OQ/PQ validation protocols, with a focus on EtO (Ethylene Oxide) sterilization and adherence to ISO 11135, FDA 21 CFR Part 820, ISO 13485, and GMP standards. The ideal candidate will have experience in vWe are seeking a Quality Validation Manager to join our team, responsible for ensuring the compliance of manufacturing equipment, processes, and sterilization protocols with industry regulations. This role involves developing, executing, and maintaining IQ/OQ/PQ validation protocols, with a focus on EtO (Ethylene Oxide) sterilization and adherence to ISO 11135, FDA 21 CFR Part 820, ISO 13485, and GMP standards. The ideal candidate will have experience in v
